Canonical Allele Identifier: PA2580103611
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1701146
ClinVar RCV Id: RCV002275482

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000034.1:p.Gln276Pro
CA377509902
NM_000043.6:c.827A>C